Neuronal abnormalities in microtubule-associated protein 1B mutant mice

被引:140
|
作者
Edelmann, W
Zervas, M
Costello, P
Roback, L
Fischer, I
Hammarback, JA
Cowan, N
Davies, P
Wainer, B
Kucherlapati, R
机构
[1] ALBERT EINSTEIN COLL MED,DEPT PATHOL,BRONX,NY 10461
[2] ALBERT EINSTEIN COLL MED,DEPT NEUROSURG,BRONX,NY 10461
[3] ALBERT EINSTEIN COLL MED,DEPT PATHOL & NEUROSCI,BRONX,NY 10461
[4] MED COLL PENN,DEPT ANAT & NEUROBIOL,PHILADELPHIA,PA 19129
[5] HAHNEMANN UNIV,PHILADELPHIA,PA 19129
[6] WAKE FOREST UNIV,BOWMAN GRAY SCH MED,DEPT NEUROBIOL & ANAT,WINSTON SALEM,NC 27157
[7] NYU,DEPT BIOCHEM,NEW YORK,NY 10016
关键词
gene targeting; ataxia; Purkinje cells; ocular abnormalities;
D O I
10.1073/pnas.93.3.1270
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Microtubules play an important role in establishing cellular architecture. Neuronal microtubules are considered to have a role in dendrite and axon formation, Different portions of the developing and adult brain microtubules are associated with different micro tubule-associated proteins (MAPs), The roles of each of the different MAPs are not well understood, One of these proteins, MAP1B, is expressed in different portions of the brain and has been postulated to have a role in neuronal plasticity and brain development, To ascertain the role of MAP1B, we generated mice which carry an insertion in the gene by gene-targeting methods, Mice which are homozygous for the modification die during embryogenesis. The heterozygotes exhibit a spectrum of phenotypes including slower growth rates, lack of visual acuity in one or both eyes, and motor system abnormalities, Histochemical analysis of the severely affected mice revealed that their Purkinje cell dendritic processes are abnormal, do not react with MAP1B antibodies, and show reduced staining with MAP1A antibodies, Similar histological and immunochemical changes were observed in the olfactory bulb, hippocampus, and retina, providing a basis for the observed phenotypes.
引用
收藏
页码:1270 / 1275
页数:6
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